PTSD (Childbirth-Related)

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Review clinical trials related to PTSD (Childbirth-Related). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Debriefing Consult for Psychiatric Symptoms After Severe Maternal Morbidity

The primary objective of this study is to determine if a maternal fetal medicine (MFM) debriefing consult six to eight weeks postpartum reduces self-reported post-traumatic stress, depression, and anxiety symptoms following a delivery complicated by severe maternal morbidity (SMM). Individuals with a delivery complicated an intensive care unit (ICU) admission and/or blood product transfusion \>4 units will be included in this study. Participants will be randomized to an intervention or control group; all participants will complete patient questionnaires that screen for post-traumatic stress disorder, depression, and anxiety. Those in the control group will receive a virtual MFM debriefing consult at six weeks postpartum and those in the intervention group will have the option for a consult at twelve weeks postpartum, after the completion of the questionnaires.

Participants needed: 52
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Cedars-Sinai Medical CenterUpdated: Jul 6, 2026Locations: 1
Eligibility criteria

Age <18 years [+2]

Status: Recruiting

The New Empowerment After eXposure to Trauma (NEXT) Study

The NEXT Study is a randomized controlled pilot examining the feasibility and acceptability of a revised perinatal PTSD protocol. This study will randomize perinatal participants with PTSD to receive NET (n=45); treatment group) and will be compared to perinatal women randomized to usual care (n=45; comparator group). The overall objective of this project is to determine the most feasible and acceptable protocol for a brief virtual perinatal PTSD intervention.

Participants needed: 106
Trial details
Age: 18-50Biological sex: FemaleType: InterventionalSponsor: Indiana UniversityUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

18 years of age or older [+3]

current severe suicide risk as determined by the Columbia Suicide Severity Ratin... [+7]

Status: Recruiting

Early Intervention for Postpartum PTSD: Comparing Written Exposure and Capnometry-Guided Breathing Therapy

The purpose of this study is to examine two early interventions, Written Exposure Therapy and Capnometry Guided Breathing, to reduce post-traumatic stress disorder (PTSD) symptoms in women after childbirth as compared to usual care.

Participants needed: 70
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Stanford UniversityUpdated: Apr 24, 2026Locations: 2
Eligibility criteria

Age ≥18 [+5]

Active psychosis or mania [+3]

Status: Recruiting

Feasibility and Efficacy of GTEP for Birth Trauma

This clinical study aims to evaluate the feasibility and initial efficacy of Group Traumatic Episode Protocol (GTEP) for reducing trauma symptoms (measured by the PCL-5 and City BiTS) for individuals following a traumatic birthing experience. A secondary aim is to evaluate the efficacy of GTEP in improving parental wellbeing (measured through the CORE-10) and parent-infant bonding (measured through the PBQ) following a traumatic birthing experience. Participants (those who have experienced a traumatic birthing experience) will complete the GTEP intervention, delivered online. They will be asked to complete outcome measures and give feedback on their experience of the group.

Participants needed: 10
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: University of BirminghamUpdated: Feb 19, 2026Locations: 1
Eligibility criteria

Aged between 18-65 years. [+7]

Women/birthing people whose baby is no longer under their care. [+2]